{"id":21232,"date":"2025-11-17T01:45:43","date_gmt":"2025-11-16T22:45:43","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/zellweger\/"},"modified":"2025-11-17T01:45:43","modified_gmt":"2025-11-16T22:45:43","slug":"zellweger","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/zellweger\/","title":{"rendered":"Zellweger Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Zellweger syndrome is a lethal disease characterized by peroxisome dysfunction, severe neurological findings, and dysmorphic face.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Severe hypotonia<\/li>\n<li>Characteristic face<\/li>\n<li>Liver dysfunction<\/li>\n<li>Convulsions<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>PEX gene mutations.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Plasma very long chain fatty acids, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Palliative care.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Metabolism Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of respiratory failure, emergency services should be consulted.<\/p>\n<p><em>This page is for general information purposes only.<\/em><\/p>","protected":false},"excerpt":{"rendered":"<p>Definition: Zellweger syndrome is a lethal disease characterized by peroxisome dysfunction, severe neurological symptoms, and dysmorphic facial features. Symptoms: Severe hypotonia, characteristic facial features, liver dysfunction, convulsions. Causes: PEX gene mutations. Diagnosis: Plasma long-chain fatty acids, genetic testing. Treatment: Palliative care. Which Clinic Should You Visit? Metabolism Clinic. What to Do in an Emergency? In case of respiratory failure [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Zellweger Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Zellweger syndrome is a lethal disease characterized by peroxisome dysfunction, severe neurological symptoms, and facial dysmorphia. Symptoms include:"},"footnotes":""},"class_list":["post-21232","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21232","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar"}],"about":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/types\/hastaliklar"}],"author":[{"embeddable":true,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/users\/1"}],"version-history":[{"count":0,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21232\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21232"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}